摘要
目的:确定额外标记染色体来源,对染色体异常患者进行明确的遗传学诊断。方法:应用比较基因组杂交(comparative genomic hybridization,CGH)和荧光原位杂交(fluorescence in situ hybridization,FISH)技术对1例小标记染色体患者进行分子细胞遗传学检测。结果:显示13号染色体近着丝粒q11-q12区有一明显扩增,提示该额外小标记染色体来源于13号染色体pter→q12。结论:CGH结合FISH技术是鉴别标记染色体来源的又一快速便捷的方法。
Objective To identify the origin of the marker chromosome in a patient with chromosome aberration, and to provide the precise genetic diagnosis. Methods hybridization (CGH) and fluorescence in situ hybridization (FISH) known small marker chromosome in this patient. Results The small from chromosome 13pter→q12. Conclusion CGH and FISH can be Comparative genomic were performed to detect the marker chromosome originated used to detect the small marker chromosome, which is convenient and quick in detecting the origin of small marker chromosome.
出处
《中南大学学报(医学版)》
CAS
CSCD
北大核心
2007年第2期264-267,共4页
Journal of Central South University :Medical Science
基金
"十五"国家攻关课题(2004BA720A02)
国家自然科学基金(30571021)~~
关键词
比较基因组杂交
荧光原位杂交
标记染色体
comparative genomic hybridization
fluorescence in situ hybridization
marker chromosome